Taiwan FDA registration ec31d9cfac9ad222806642c2ac441172
"Luci" Oropharyngeal airway tube (unsterilized)
TW: "路希" 口咽氣道管(未滅菌)
Taiwan·Risk Class 1·WILLY RUSCH GMBH·Registered Jun 19, 2012 – Jun 19, 2022CancelledRegistration details
- Analysis ID
- ec31d9cfac9ad222806642c2ac441172
- Customs Code
- DHA04401184302
Company information
- Manufacturer
- WILLY RUSCH GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5110 Oropharyngeal airway tubes
- Import Information
- import
Dates and status
- Registration Date
- Jun 19, 2012
- Expiry Date
- Jun 19, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Luci" Oropharyngeal airway tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ec31d9cfac9ad222806642c2ac441172 and manufactured by WILLY RUSCH GMBH. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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